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Familial chilblain lupus

MONDO:0018827

An instance of Chilblain lupus that is caused by an inherited modification of the individual's genome.

Also known as: hereditary Chilblain lupus, hereditary chilblain lupus

46 clinical trials for this condition and its sub-types, 2 tagged with Familial chilblain lupus itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary disorder of connective tissue (1314) ↑ Hereditary skin disorder (885) ↑ Type 1 interferonopathy of childhood (19) ↑ Chilblain lupus (3)

Sub-types of Familial chilblain lupus

Chilblain lupus 1 0 trials
Chilblain lupus 2 0 trials

Including sub-types (46) Tagged with Familial chilblain lupus (2)

Trials to join now! 1 Not yet finished but already full! 1

New pill aims to tame rare immune diseases

Disease control Ongoing

This early-stage trial tests an experimental drug called BI 3000202 in 16 adults with rare type 1 interferonopathies, such as Aicardi-Goutières syndrome. Participants take a low dose for 4 weeks, then a higher dose for 36 weeks. The main goal is to see if the drug is safe and how…

Phase 1 • Sponsor: Boehringer Ingelheim • Aim: Disease control

Last updated Sep 17, 2026 00:00 UTC